DHEA

Manufacturer: Deseret Biologicals, Inc. | Apotheca Company
Effective date: 2024-09-23
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 02:28:02

Label at a glance#

ProductDHEA

Active ingredientPRASTERONE

Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • fatigue • low energy These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Contacts and useful links#

PhoneLabel contact800-827-8204

Websitewww.desbio.com

www.desbio.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

DHEA (DEHYDROEPIANDROSTERONE) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

PURPOSE:

OTC - PURPOSE SECTION

DHEA (DEHYDROEPIANDROSTERONE) - Fatigue, Low Energy

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• fatigue • low energy

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

Tamper Evident: Sealed for Your Protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

DHEA

Homeopathic

NDC 43742-0564-1
1 FL OZ (30 ml)

DHEA

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
86ca2ee7-106a-420e-9137-a9ec1af5dbc1	Product name	1	20170110

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43742-0564-1	DHEA	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43742-0564	DHEA (DHEA (DEHYDROEPIANDROSTERONE)) LIQUID [DESERET BIOLOGICALS, INC.]	6	Current NDC, Legacy NDC, 1 package rows	20240925_d6edd874-495c-4eb5-bf3d-72c2ee41fc88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
PRASTERONE	ACTIVE INGREDIENT	459AG36T1B	2
PRASTERONE	ACTIVE MOIETY	459AG36T1B	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

DHEA
DHEA (Dehydroepiandrosterone)
PRASTERONE
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43742-0564	43742-0564-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PRASTERONE	459AG36T1B	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DHEA	DHEA (DEHYDROEPIANDROSTERONE)	Deseret Biologicals, Inc.	d6edd874-495c-4eb5-bf3d-72c2ee41fc88	2024-09-23	Warnings	Exact identifier ndc (package): 43742-0564-1 ndc (product): 43742-0564 ndc11 (package): 43742056401 spl id: a77dc7d0-2782-45e4-ae58-1625a00f9c41 spl set id: d6edd874-495c-4eb5-bf3d-72c2ee41fc88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.